ATP2B1 (Q4654809)

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protein-coding gene in the species Homo sapiens

ATPase, Ca++ transporting, plasma membrane 1
PMCA1
PMCA1kb
ATPase plasma membrane Ca2+ transporting 1

Language	Label	Description	Also known as
English	ATP2B1	protein-coding gene in the species Homo sapiens	ATPase, Ca++ transporting, plasma membrane 1 PMCA1 PMCA1kb ATPase plasma membrane Ca2+ transporting 1

Statements

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000070961

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ATPase plasma membrane Ca2+ transporting 1

1 reference

6 July 2017

UniProt protein ID

Plasma membrane calcium-transporting ATPase 1

1 reference

UniProt protein ID

19 March 2016

language of work or name

genetic association

coronary artery disease

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_3393&ncbiId=490

http://www.genome.gov/gwastudies/index.cfm?gene=ATP2B1

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease

25 May 2020

arterial hypertension

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10763&ncbiId=490

http://www.genome.gov/gwastudies/index.cfm?gene=ATP2B1

Genome-wide association study of blood pressure and hypertension

25 May 2020

human chromosome 12

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

89588049

human chromosome 12

genomic assembly

genome assembly GRCh38

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

89981828

human chromosome 12

genomic assembly

Genome assembly GRCh37

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

89709300

human chromosome 12

genomic assembly

genome assembly GRCh38

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

90103077

human chromosome 12

genomic assembly

Genome assembly GRCh37

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

cytogenetic location

12q21.33

1 reference

13 January 2018

55597

1 reference

6 January 2018

Gene Atlas image

PBB GE ATP2B1 215716 s at fs.png
732 × 530; 12 KB

0 references

PBB GE ATP2B1 212930 at fs.png
732 × 530; 11 KB

0 references

PBB GE ATP2B1 209281 s at fs.png
732 × 530; 11 KB

0 references

1 reference

HomoloGene build68

55597

1 reference

HomoloGene build68

55597

1 reference

HomoloGene build68

55597

1

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

Brodmann area 23

2

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

3

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

4

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

external globus pallidus

5

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

secondary oocyte

6

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

superior frontal gyrus

7

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

orbitofrontal cortex

8

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

stromal cell of endometrium

9

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

Region I of hippocampus proper

10

1 reference

19 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000070961

http://identifiers.org/ncbigene/490

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

1 reference

6 January 2018

Ensembl gene ID

ENSG00000070961

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

Ensembl transcript ID

ENST00000552275

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000261173

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000359142

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000393164

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000428670

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000549585

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000549727

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000550716

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000551009

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000551310

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

ENST00000635033

1 reference

Ensembl Release 91

Ensembl gene ID

ENSG00000070961

0 references

HGNC gene symbol

1 reference

6 January 2018

1 reference

6 January 2018

Microsoft Academic ID

0 references

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(2 entries)

enwiki ATP2B1
ukwiki ATP2B1

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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